Data / Drug companies / Thrombopoietin Receptor Agonist
Thrombopoietin Receptor Agonist drugs: 3 drugs from 17 companies in the FDA NDC directory
Thrombopoietin Receptor Agonist is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 75 products in this class from 17 companies, covering 3 drugs by generic name. The main marketing category is generic drugs (ANDA), and the newest product started marketing on October 15, 2026.
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- 17Companies
- 75Products
- 3Drugs by generic name
Drugs in the Thrombopoietin Receptor Agonist class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Eltrombopag | 45 | 11 |
| Eltrombopag olamine | 27 | 7 |
| Romiplostim | 3 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Teva Pharmaceuticals, Inc. | 8 | tablet, film coated | Generic drugs (ANDA) | September 17, 2026 |
| Camber Pharmaceuticals, Inc. | 6 | tablet, film coated; powder, for suspension | Generic drugs (ANDA) | May 13, 2025 |
| Novartis Pharmaceuticals Corporation | 6 | tablet, film coated; powder, for suspension | New drug applications (NDA) | September 27, 2018 |
| Amerisyn LLC | 4 | tablet, film coated | Generic drugs (ANDA) | June 30, 2026 |
| Amneal Pharmaceuticals NY LLC | 4 | tablet, film coated | Generic drugs (ANDA) | January 15, 2026 |
| Amneal Pharmaceuticals NY LLC | 4 | tablet, film coated | Generic drugs (ANDA) | January 15, 2026 |
| AvKARE | 4 | tablet, film coated | Generic drugs (ANDA) | February 16, 2026 |
| Biocon Pharma Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | September 9, 2026 |
| Dr. Reddy's Laboratories Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | March 17, 2026 |
| Hikma Pharmaceuticals USA Inc. | 4 | tablet | Generic drugs (ANDA) | April 24, 2026 |
| Novadoz Pharmaceuticals LLC | 4 | tablet, film coated | Generic drugs (ANDA) | January 14, 2026 |
| Quallent Pharmaceuticals Health LLC | 4 | tablet, film coated | Generic drugs (ANDA) | October 15, 2026 |
| Somerset Therapeutics, LLC | 4 | tablet, film coated | Generic drugs (ANDA) | January 14, 2026 |
| XLCare Pharmaceuticals, Inc. | 4 | tablet, film coated | Generic drugs (ANDA) | August 7, 2025 |
| Zydus Lifesciences Limited | 4 | tablet | Generic drugs (ANDA) | January 14, 2026 |
| Zydus Pharmaceuticals USA Inc. | 4 | tablet | Generic drugs (ANDA) | January 14, 2026 |
| Amgen, Inc | 3 | injection, powder, lyophilized, for solution | Biologics (BLA) | August 2, 2019 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 56 | 74.7% |
| Tablet | 12 | 16% |
| Powder, for suspension | 4 | 5.3% |
| Injection, powder, lyophilized, for solution | 3 | 4% |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.